HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylurea → Ethyl 2-(ethylamino)-4-(trifluoromethyl)-5-oxazolecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylurea | HCID 12254 | — |
| Reactant | Ethyl 2-chloro-4,4,4-trifluoro-3-oxobutanoate | HCID 2737165 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(ethylamino)-4-(trifluoromethyl)-5-oxazolecarboxylate | HCID 20064763 | 63.4% |
Reaction Steps
By the procedures of Example 4, 5.3 g (60 mmol) of ethyl urea was reacted with 10.9 g (50 mmol) of ethyl 2-chloro-4,4,4-trifluoroacetoacetate at 140°-150° C. for 24 hours. The product mixture was treated with methylene chloride, washed with water, dried and concentrated. The residue was recrystallized from methylcyclohexane to yield 8.0 g of crystal product (m.p.=89°-90° C.) identified in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05000775 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-9e1e3e16ecdd485ca884f66312479be6 |
| Source note | uspto-grants-1991_03 |